| Health / Medical Topics |
GRK1 wt Allele
Human GRK1 wild-type allele is located within 13q34 and is approximately 4 kb in length. This allele, which encodes rhodopsin kinase protein, plays a role in the deactivation of rhodopsin. Heritable defects in the GRK1 gene cause Oguchi disease 2. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene is involved in sensory transduction necessary for vision.
A descriptive term that is used in anatomic pathology and refers to the gritty appearance of the cut surface of a…
An antifungal agent derived from the mold Penicillium griseofulvum that is used to treat fungal infections of the skin and nails. Griseofulvin…
A rare, autosomal recessive genetic syndrome caused by mutations in the RAB27A gene. It is characterized by hypopigmentation of the skin,…
The ability to hold or grasp.
Human GRIN2B wild-type allele is located in the vicinity of 12p12 and is approximately 419 kb in length. This allele, which encodes…
